5-Aroyl 6-chloro or 6-bromo 1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-di-carboxylates

ABSTRACT

5-Substituted-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids of the formula ##STR1## wherein: X is hydrogen, lower alkyl, chloro or bromo; Ar is a moiety selected from the group consisting of ##STR2## in which: Y is oxygen or sulfur; 
     R is hydrogen, methyl, chloro, or bromo, the R substitution being at the 3, 4 or 5 position of the ring; 
     R 1  is hydrogen, lower alkyl, lower alkoxyl, lower alkoxycarbonyl, lower alkylcarbonyl, fluoro, chloro or bromo, the R 1  substitution being at any available position in the ring; 
     R 2  is hydrogen or lower alkyl; 
     are prepared by β-decarboxylation of the corresponding dialkyl-1,1-dicarboxylates. Certain substituted pyrroles are useful as intermediates for preparing the compounds of formula I.

This is a division of application Ser. No. 272,818 filed June 11, 1981, U.S. Pat. No. 4,347,186, which is a continuation-in-part of Ser. No. 198,552, filed Oct. 20, 1980, U.S. Pat. No. 4,347,186.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to a process for preparing 5-aroyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylic acids of the formula ##STR3## by decarboxylation of the corresponding 1,1-dicarboxylates. This invention also related to a process for the preparation of the 1,1-decarboxylates and novel intermediates therein.

2. Related Disclosures

The "end-products" of Formula (I) with the exception of those wherein R¹ is carboxyl, lower alkoxycarbonyl or lower alkylcarbonyl, have been previously described. The Ar moiety, as will be described herein below, is shown as ##STR4##

U.S. application Ser. No. 157,719, filed June 9, 1980 discloses those embodiments of the present invention wherein X is equal to chloro or bromo.

The preparation of the above is disclosed by methods other than those disclosed herein.

The compounds of Formula (I) are useful as anti-inflammatory agents, analgesic agents, platelet aggregation inhibitors, fibrinolytic agents, and as smooth muscle relaxants. They can be used both prophylactically and therapeutically, as disclosed in U.S. Ser. No. 157,719, U.S. Pat. Nos. 4,087,539, 4,089,969, and 4,097,579 which are incorporated herein by reference.

SUMMARY OF THE INVENTION

One aspect of the invention herein relates to preparation of the compounds of Formula (I) by decarboxylating the corresponding dialkyl 5-substituted-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylates of the formula ##STR5## wherein: X is hydrogen, lower alkyl, chloro or bromo; Ar is a moiety selected from the group consisting of ##STR6## in which: Y is oxygen or sulfur;

R is hydrogen, methyl, chloro, or bromo, the R substitution being at the 3, 4 or 5 position of the ring;

R¹ is hydrogen, lower alkyl, lower alkoxycarbonyl, lower alkoxycarbonyl, lower alkylcarbonyl, fluoro, chloro or bromo, the R¹ substitution being at any available position in the ring;

R² is hydrogen or lower alkyl;

and R³ is hydrogen or lower alkyl,

to compounds of Formula I, by treating them with acid or preferably by treating with base and subsequently treating with acid. Said conversion may be represented schematically: ##STR7##

Another aspect of this invention relates to overall synthesis of compounds of formula I and preparation of compounds of formula II.

The intermediate compounds in said overall process are new. Therefore, in another aspect, the present invention relates to these novel compounds, which are useful as intermediates in the process herein and are set forth below.

DETAILED DESCRIPTION OF THE INVENTION Definitions

As used herein,

"lower alkyl" means a branched or unbranched saturated hydrocarbon chain containing from one to four carbon atoms;

"lower alkoxyl" means --OR wherein R is lower alkyl as herein defined;

"lower alkoxycarbonyl" means ##STR8## wherein R is lower alkyl as herein defined; "lower alkylcarbonyl" means ##STR9## wherein R is lower alkyl as herein defined; "strong mineral acid" means an inorganic water soluble, easily dissociable Bronsted Lowry acid, such as hydrochloric, sulfuric, phosphoric and the like;

"strong mineral base" means an inorganic water soluble, base with a pk_(b) less than about 5, such as sodium hydroxide, sodium carbonate, potassium bicarbonate and the like.

"optionally substituted phenyl" means a phenyl group which may or may not be substituted with a moiety selected from the group consisting of halo and lower alkyl.

PREPARATION OF COMPOUNDS OF FORMULA II

A schematic of the conversion of compounds of Formula A, i.e. pyrrole or of the 3-lower alkyl pyrroles (wherein X" is hydrogen or lower alkyl and X' is chloro or bromo), to compounds of Formula II is shown in Reaction Scheme I. ##STR10##

(In formulas B_(s) and B_(s) ', A represents an anion, preferably halide, and most preferably chloride.)

The intermediates B through H may be isolated, if desired, using conventional techniques, including but not limited to, filtration, distillation, crystallization, chromatography and the like as stated hereinabove. Such intermediates may be characterized using conventional means, including physical constants and spectral characteristics.

As seen from Reaction Scheme I, the process converges at compounds of formula C, but then diverges into 3 alternative pathways, a, b and c (which, at times overlap) and then converges to a common intermediate at compounds of Formula H. Step 6 is then congruent with respect to these alternatives.

In those embodiments wherein X is halo, i.e. chloro or bromo, preparation of the compound of Formula C proceeds via an intermediate dimethylsulfonium-substituted pyrrole which permits substitution of the chloro or bromo into the proper position of the pyrrole nucleus. This set of procedures is shown as steps 1_(1x), 1_(2x), 1_(3x), and 2_(x) on Reaction Scheme 1.

Preparation of compounds of Formula B, accomplished herein in Steps 1₁ and 1₂ has been described elsewhere: Matteson et al, J. Org. Chem. 22:1500 (1957); Japanese Pat. No. 53/025,559.

However, in the present invention, improved yields were obtained by a new process which comprises treating the appropriate pyrrole or 3-alkyl pyrrole with a reagent formed from dimethylsulfide and an N-halosuccinimide.

(Other dialkyl sulfides may also be used, but there is no advantage to doing so, as the alkyl sulfide group will be lost during the subsequent steps in the process.) Steps 1₁ and 1_(1x) are, of course, identical. To carry out either, a solution of a n-halosuccinimide, preferably n-chlorosuccinimide, in an inert solvent such as, for example, dichloromethane, is cooled to a temperature of between about -60° C. and +5° C. under an inert atmosphere such as, for example, nitrogen, argon or helium. To this, between an equimolar amount and about a 5 mol excess, preferably a 2-3 mol excess of dimethylsulfide is added, similarly dissolved in an inert solvent, over a period of between about 10 minutes to 3 hours, preferably 1 to 11/2 hours. After an additional time period at this temperature, between about 10 minutes and 3 hours, preferably 1 to 11/2 hours, a solution of pyrrole in an amount equimolar to the n-chlorosuccinimide, dissolved in the same inert solvent as used for the previous two reagents, is added over a period of between about 10 minutes to 3 hours, preferably 1 hour to 11/2 hours at the same temperature as has been maintained so far. The solution is then stirred for another time period of 10 minutes to 5 hours, preferaly about 11/2 to 3 hours, and an excess of a precipitating solvent such as, for example, diethylether is added until precipitation takes place or solvent is evaporated, to yield the compound of Formula B_(s) --the methylchloride (for example) salt of the compound of Formula B. The compound of Formula B is formed by pyrolysis, either by heating in vacuo and collecting product as distillation occurs, or by heating in the presence of solvent and collecting the product by subsequent distillation. (Of course, if step 1_(2x) is to be done, the conversion to Formula B would be premature.)

In those embodiments wherein X is hydrogen or lower alkyl, the conversion of B to C in step 2 is substantially the process described in U.S. Pat. Nos. 4,087,539; 4,089,969 and 4,097,579, which are incorporated herein by reference. The procedures as described therein may be modified by using ether dialkylamines, such as methyl ethyl amine, ethyl n-propyl amine and the like to form the aroylamides. The resulting aroylamides may then be substituted for the aroyldimethylamides in the same procedures. Additionally, aroyl halides may be used directly, obviating the need for phosphorus oxychloride or other analogous halogenating agent. However, the resulting compounds of Formula C are new.

In those embodiments wherein X is chloro or bromo, the "intermediate" of formula B_(s) is first halogenated to give the compound of formula B_(s) ', before conversion to the free sulfide form of formula B'.

In this process, in Step 1_(2x), the dimethyl sulfonium salt is halogenated with a suitable positive halogen donor such as, for example, sulfuryl chloride or a halogen, preferably sulfuryl chloride and the 4-halogenated dimethyl sulfonium salt which results is then decomposed to the corresponding methylthioderivative, of formula B', which is unstable. In this process, the methylsulfonium salt as prepared in step 1_(1x) is dissolved in an inert solvent such as, for example, dichloromethane and then cooled to a temperature of about -90° C. to -50° preferably, between about -80° and -70° C. To this solution is added an approximately two-fold excess of halogenating agent such as, for example, sulfuryl chloride, or halogen, preferably sulfuryl chloride and the solution continued to be stirred at the previous low temperature for approximately 6 hours to 24 hours, preferably overnight. The intermediate halogenated sulfonium salt may be collected by filtration and purified if desired, and is then decomposed by heating with an inert solvent such as, for example, toluene, xylene, or other hydrocarbon solvent, preferably xylene in an inert atmosphere for about 10 minutes to 30 minutes, preferably about 15 minutes.

Since the resulting methylthio compound is unstable, it is converted immediately into the compound of Formula C by reacting it with a previously prepared solution. The solution contains the appropriate N,N-dimethyl aroyl compound of the formula ArCON(CH₃)₂ in approximately equimolar quantity to the pyrrole to be aroylated along with phosphorus oxychloride in, again, approximately equal quantity, in an inert solvent such as, for example, dichloromethane, 1,2-dichloroethane, or other halogenated hydrocarbon, preferably 1,2-dichloroethane. (Vilsmeier-Haack Reagent.)

The Vilsmeier-Haack Reagent is then added to the methylthiopyrrole derivative, and the mixture heated at a temperature of about 50° C. to about 120° C., preferably reflux temperature of the solution under an inert atmosphere for approximately 8 hours to 48 hours, preferably 20 to 28 hours. The product of formula C, is then isolated by conventional means.

This process is that referenced hereinabove to U.S. Pat. Nos. 4,087,539, 4,089,969 and 4,097,579 in setting forth Step 2.

As stated in the description of step 2 hereinabove, other aroyl amides may be used to form the compounds of formula C, however there is no particular advantage in so doing.

Steps 3a, 3b and 4c are each effected in the same manner as each other. The subject pyrrole derivative is treated with an excess of an alkali metal hydride or other strong base, preferably sodium hydride under an inert atmosphere e.g. nitrogen, neon or argon, preferably argon, until reaction is complete. This time may range from 10 minutes to 10 hours, but is ordinarily in the range of 1-2 hours. The reaction takes place at about 0°-40°, but preferably at room temperature i.e. 15°-25°. Operable solvents include any aprotic organic polar solvent, e.g., DME, diglyme, DMF and the like; preferably DMF.

After the treatment with the hydride, compound J i.e. spiro[2,5]-5,7-dioxa-6,6-dimethyloctane-4,8-dione, prepared according to Singh et al, J. Org. Chem. 40:2969 (1975) is added in slight excess and the temperature is raised to about 40°-80°, preferably 50°-60°, and the mixture is allowed to react for about 1-10 hours or to completion. The product, a compound of Formula D (Steps 3a or 3b) or Formula G (Step 4c) may be isolated, preferably as the salt.

Analogous spiro cyclopropyl compounds, with the general formula ##STR11## wherein each R may independently be lower alkyl, may also be used. These compounds may be prepared in a manner similar to that for spiro[2,5]-5,7-dioxa-6,6-dimethyloctane-4,8-dione by substituting other ketones for acetone to form the dioxyketal ring. Thus, for example, spiro[2,5]-5,7-dioxa-6,6-diethyl-octane-4,8-dione, spiro[2,5]-5,7-dioxa-6-methyl-6-ethyl-octane-4,8-dione, and 2-spiro[2,5]-5,7-dioxa-6-methyl-6-propyl-octane-4,8-dione, may be prepared using 3-pentanone, methyl ethyl ketone (2-butanone) and 2-pentanone respectively. However, there is no particular advantage in varying the 6,6-substitution, since subsequent steps in the overall process remove these groups, and ease of removal is not enhanced by such variation. Therefore, the preferred method is to employ spiro[2,5]-5,7-dioxa-6,6-dimethyloctane-4,8-dione.

Steps 4a, 5b and 5c are carried out similarly to each other. In each case the cyclic diester dissolved in a suitable solvent, e.g. an alcohol, is converted to the corresponding dialkyl dicarboxylate or dicarboxylic acid by treatment with a suitable alcohol in the presence of acid. In a preferred embodiment the subject compound is dissolved in methanol and treated with methanol previously saturated with HCl at about 0°-80°, preferably 20°-60° for about 5 minutes to 5 hours, preferably 10 minutes to 40 minutes. The dimethyl or other dialkyl ester may then be recovered by suitable conventional techniques.

Steps 5a, 3c, and 4b all represent the oxidation of the methyl thiopyrrole to the methyl sulfonylpyrrole. An excess of oxidizing agent, e.g. peroxide, permanganate, or peracid preferably m-chloroperbenzoic acid in excess, and preferably in an approximately 2:1 molar ratio to the subject compound is used. The reaction can be done at low temperature, about -10° to +15°, preferably 0° C. in a non-polar, aprotic organic solvent, e.g. chloroform, dichloromethane or dichloroethane, preferably dichloromethane. The reaction time may vary from about 15 minutes to 10 hours; usually it is in the range of 2-3 hours. The product is then recovered using techniques familiar to those skilled in the art.

The sequences 3a, 4a, 5a; 3b, 4b, 5b; and 3c, 4c, 5c all converge at compounds of formula H, the dimethyl 1-pyrrolyl malonate derivative of the 5-aroyl pyrrole. Cyclization to the corresponding pyrrolo[1,2-a]pyrrole compound of Formula II takes place in step 6.

To carry out step 6, the subject compound is dissolved in an aprotic organic polar solvent, preferably dimethylformamide and treated with a slight excess of an alkali metal hydride, preferably sodium hydride in mineral oil. When the formation of the salt of the malonate derivative has been completed, at room temperature, as shown by the cessation of hydrogen evolution, cyclization is effected by heating to about 30°-150° for about 10 minutes to 10 hours, preferably to 50°-110° for 4-6 hours. All of these operations are carried out in an inert atmosphere, preferably under nitrogen. The mixture is then cooled to about 5°-40°, preferably room temperature (15°-25°) and the solution made acidic, preferably by addition of 10% hydrochloric acid. The product of Formula II may then be recovered.

The compounds of Formula II are then converted to the corresponding 5-aroyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids as described hereinbelow.

THE CONVERSION OF COMPOUNDS OF FORMULA II TO COMPOUNDS OF FORMULA I

The conversion herein consists of treatment with base to accelerate ester hydrolysis, followed by treatment with acid to effect decarboxylation.

In the special case where R³ is hydrogen, treatment with base is unnecessary, and the conversion can be carried out in the presence of acid only. Where R³ is lower alkyl, it is possible, but not particularly desirable to carry out the entire conversion under acid conditions; the preferred method is to hydrolyze the esters first by treatment with base, and then decarboxylate in acid.

The conditions of treatment with base and acid to effect hydrolysis and decarboxylation are familiar to those skilled in the art for decarboxylation of β-dicarboxylic acid esters. For hydrolysis under basic conditions, the use of a strong base, preferably a mineral base, e.g., potassium hydroxide, sodium hydroxide, lithium hydroxide, and the like, in the presence of water is preferred. Advantageously, water miscible organic solvents, e.g., 2-methoxyethanol, methanol, ethanol, ethylene glycol, dimethylsulfoxide, and the like are used to facilitate solution of the reactants. The reaction is preferably carried out under an inert atmosphere, e.g., nitrogen, argon, and the like. The reaction times and temperatures are not critical and depend, as will be apparent to those skilled in the art, on the reactants (and other ingredients of the reaction mixture) employed. Thus the reaction time can be from about 5 minutes to about 2 hours, with 30 minutes to 1 hour being preferred; and the reaction temperature from about 60° C. to reflux temperature with 70° C. to reflux temperature being preferred.

Subsequent treatment with acid is effected preferrably with a strong mineral acid, e.g., phosphoric acid, sulfuric acid, hydrochloric acid, hydrobromic acid, and the like in the presence of water, with or without the presence of an organic acid, e.g., acetic acid, formic acid, propionic acid, and the like. If desired other organic solvents miscible with the mineral acid (and the water and the organic acid, if the latter is used) can be used. Suitable organic solvents are ethyl acetate, methanol, ethanol, ethylene glycol, dimethylsulfoxide, dioxane, tetrahydrofuran, ethylene glycol dimethyl ether (glyme), diethylene glycol dimethyl ether (diglyme), and the like. The reaction may be carried out under an inert atmosphere, e.g., nitrogen, argon, and the like. The reaction times and temperatures are not critical and depend, as will be apparent to those skilled in the art, on the reactants and other ingredients of the reaction mixture) employed. Thus, the reaction time can be from instanteous to about 10 hours with one minute to 5 minutes being preferred; and the reaction temperature from about 10° C.-100° C., preferably 15°-30° C.

Isolation, separation, and purification of the desired compound of Formula (I) from the reaction mixture containing it can be effected by any suitable separation or purification procedure, such as, for example, extraction, filtration, evaporation, distillation, crystallization, thin-layer chromatography, or column chromatography, high pressure liquid chromatography, and the like, or a combination of these procedures. Illustrations of suitable isolation, separation and purification procedures can be had by reference to the Examples herein below. However, other isolation, separation and isolation procedures, could of course, also be used.

NOVEL INTERMEDIATES

The compounds of formula B_(s) ', C, D, E, F, G, H and II are novel, and are useful as intermediates in preparing compounds of formula (I) which are therapeutically useful as discussed hereinbefore.

PREFERRED EMBODIMENTS

A set of preferred embodiments of the present invention is composed of those wherein the decarboxylation of the compounds of formula II is effected by treating said compounds with acid, especially strong mineral acid, or more preferably by treating said compounds with base, followed by acid, and most preferably with strong mineral base followed by strong mineral acid.

The sequences 1, 2, 3a, 4a, 5a, 6 and 1, 2, 3b, 4b, 5b, 6 in the preparation of the compound of formula II appear slightly superior to the sequence 1, 2, 3c, 4c, 5c, 6. However, the latter sequence is certainly perfectly practicable.

Another set of preferred embodiments is that wherein X is hydrogen, methyl or chloro and Ar is 2-theonyl, 2-furoyl, 2-pyrroyl or optionally substituted phenyl.

The conversion of step 6 is best carried out by treating a compound of formula H with an alkali metal hydride in an aprotic solvent.

The conversions of steps 5a, 4b, and 3c are best carried out by treating compounds of formulas F, D and C, respectively, with a perbenzoic acid.

The following examples illustrate the embodiment of the present invention, and should not be construed to limit it.

EXAMPLE 1 Preparation of 2-methylthiopyrrole (Step 1)

A. To a stirred solution of N-chlorosuccinimide (10.0 g, 0.075 moles) in dry dichloromethane (100 ml), cooled to 0°, was added a solution of dimethylsulfide (4.67 g, 0.075 moles) in dichloromethane (50 ml) at a rate such that the reaction temperature did not exceed 5°. When the addition was completed, the solution was cooled to -30° and pyrrole (5.04 g, 0.075 moles) was added slowly. The temperature was then allowed to rise to 20°, and the dichloromethane was removed in vacuo. The residue thus obtained was placed in a distillation flask and heated in vacuo in an oil bath. The fraction bp. 60°-65°/30 mm (41% yield), which contained the resulting 2-methylthiopyrrole was collected.

B. In a similar manner:

3-n-butylpyrrole,

3-i-propylpyrrole, and

3-methylpyrrole

may be converted to:

4-n-butyl-2-methylthiopyrrole,

4-i-propyl-2-methylthiopyrrole, and

4-methyl-2-methylthiopyrrole, respectively.

EXAMPLE 1A Preparation of dimethyl 2-pyrrolylsulfonium chloride (Step 1_(1x))

To a solution of N-chlorosuccinimide (40 g, 0.3 moles) in anhydrous dichloromethane (3 l), cooled to -30° to -40° C. and maintained in a nitrogen atmosphere, was added, with good stirring, α solution of dimethyl sulfide (20.5 g, 0.66 moles) in dichloromethane (125 ml) over a 1 hour period, the temperature being maintained at -30° to -40° C. After a further hour at this temperature, a solution of pyrrole (20 g, 0.3 moles) in dichloromethane (125 ml) was added over a 1 hour period maintaining a temperature of -30° to -40° C. The solution was stirred for a further 2 hours at -30° to -40° C. and then ether (ca 6 l) was added with strong agitation until the precipitation of the product was complete. The solid was collected by filtration, washed three times with ether and dried in vacuo to give a white solid of dimethyl 2-pyrrolylsulfonium chloride (40 g, 83%) which after crystallization from dichloromethane had mp 115°-116° C. dec.

UV: 221, 249 nm (ε 5130, 1020).

IR: (KBr) 3455, 3340, 3140, 1626, 1550 cm⁻¹. NMR: (D₂ O) T-60,

3.18 (s, 6H, (CH₃)₂ S), 6.44 (dd, 1H, J₃,4 =4.1, J₄,5 =2.5, H-4), 7.12 (dd, 1H, J₃,4 =4.1, J₃,5 =1.7, H-3), 7.37 (dd, 1H, J₄,5 =2.5, J₃,5 =1.7, H-5).

Calcd for C₆ H₁₀ ClNS: C, 44.02; H, 6.11. Found: C, 43.82; H, 5.94.

EXAMPLE 2 Preparation of 5-benzoyl-2-methylthiopyrrole (Step 2)

A solution of N,N-dimethylbenzamide (237 g) in anhydrous 1,2-dichloroethane (60 ml) containing phosphorus oxychloride (2.43 g) was boiled under reflux, in a nitrogen atmosphere, for 0.75 hour. To the cooled solution was added 2-methylthiopyrrole (0.9 g) in 1,2-dichloroethane (40 ml) and heating at reflux was recommenced and maintained for 1 hour. The reaction progress was followed by TLC [silica gel, dichloromethane-ethyl acetate (97:3)] which showed that the reaction was complete in 30 minutes. The reaction was cooled, sodium acetate (5.41 g) in water (80 ml) was added, and the mixture was heated at reflux temperature (nitrogen atmosphere) for 1.5 hours. The organic phase was separated, combined with a dichloromethane extract of the aqueous phase and the combined organic phases were washed with water and dried. The solvent was removed in vacuo and the residue was subjected to column chromatography on silica gel. The product was eluted with dichloromethane-hexane (1:1) and on crystallization from methanol, 2-methylthio-5-benzoylpyrrole (1.19 g, 79 %), m.p. 106°-108°, was obtained with the following properties:

UV: (MeOH) 249, 340 nm(8510, 15,100).

IR: (CHCl₃) 3420,3215, 1610, 1554, 1535 cm⁻¹.

NMR: (CDCl₃):

2.41 (s, 1H), 6.16 (m, 1H), 6.73 (m, 1H), 7.38 (m, 3H), 7.78 (m, 2H), 10.16 (m, 1H),

Calcd. for C₁₂ H₁₁ NOS: C, 66.33; H, 5.10; N, 6.44. Found: C, 66.58; H, 5.10; N, 6.36.

B. Substituting the 4-alkyl 2-methylthiopyrroles listed in part B of Example 1 for 2-methylthiopyrrole, and using a similar procedure to that in Part A of this example, one obtains, respectively,

5-benzoyl-4-n-butyl-2-methylthiopyrrole,

5-benzoyl-4-i-propyl-2-methylthiopyrrole, and

5-benzoyl-4-methyl-2-methylthiopyrrole.

C. Substituting, in the procedure of Part A of this example, for N,N-dimethylbenzamide,

N,N-dimethyl 3-thenoylamide,

N,N-dimethyl 2-furoylamide,

N,N-dimethyl 2-thenoylamide,

N,N-dimethyl 3-chloro-2-furoylamide,

N,N-dimethyl 4-bromo-2-furoylamide,

N,N-dimethyl 5-methyl-2-furoylamide,

N,N-dimethyl 4-methyl-2-thenoylamide,

N,N-dimethyl 1-butyl-2-pyrrolylamide,

N,N-dimethyl 1-methyl-2-pyrroylamide,

N,N-dimethyl 2-pyrroylamide,

N,N-dimethyl 4-chlorobenzoylamide,

N,N-dimethyl 3-methoxybenzoylamide,

N,N-dimethyl 2-ethoxycarbonylbenzoylamide,

N,N-dimethyl 2-fluorobenzoylamide,

N,N-dimethyl 3-ethylbenzoylamide,

N,N-dimethyl 4-n-ethylcarbonylbenzoylamide,

one obtains, respectively

5-(3-thenoyl)-2-methylthiopyrrole,

5-(2-furoyl)-2-methylthiopyrrole,

5-(2-thenoyl)-2-methylthiopyrrole,

5-(3-chloro-2-furoyl)-2-methylthiopyrrole,

5-(4-bromo-2-furoyl)-2-methylthiopyrrole,

5-(5-methyl-2-furoyl)-2-methylthiopyrrole,

5-(4-methyl-2-thenoyl)-2-methylthiopyrrole,

5-(1-butyl-2-pyrrolyl)-2-methylthiopyrrole,

5-(1-methyl-2-pyrroyl)-2-methylthiopyrrole,

5-(2-pyrroyl)-2-methylthiopyrrole,

5-(4-chlorobenzoyl)-2-methylthiopyrrole,

5-(3-methoxybenzoyl)-2-methylthiopyrrole,

5-(2-ethoxycarbonylbenzoyl)-2-methylthiopyrrole,

5-(2-fluorobenzoyl)-2-methylthiopyrrole,

5-(3-ethylbenzoyl)-2-methylthiopyrrole, and

5-(4-n-ethylcarbonylbenzoyl)-2-methylthiopyrrole.

EXAMPLE 2A 2-Methylthio-4-chloropyrrole (Steps 1_(2x) and 1_(3x))

The sulfonium salt prepared in Example 1A (25 g, 0.152 moles) was dissolved in dry dichloromethane (3.2 l) at room temperature and then the solution was cooled to -76° C. To the well stirred solution was added sulfuryl chloride (18.2 ml, 0.305 moles) and this solution was left stirring at -76° C. for 8 hours. The product was then precipitated in the cold by the addition of ether (4 l) with good stirring. The product, dimethyl 4-chloro-2-pyrrolylsulfonium chloride, was collected by filtration and dried in vacuo to give a white solid (16.8 g, 56%) which was crystallized from methanol-ether for analysis.

mp: 150°-200° dec.

UV: 210, 222, 258 nm (ε 4680, 5890, 8320).

IR: (KBr) 3400, 1667, 1602, 1582 cm⁻¹.

NMR: (D₂ O), 3.37 (s, 6H, (CH₃)₂ S, 7.24 (d, 1H, J₃,5 =1.4, H-3 or H-5), 7.49 (d, 1H, J₃,5 =1.4, H-5 or H-3).

Calcd for C₆ H₉ Cl₂ NS: C, 36.37; H, 4.57. Found: C, 36.15; H, 4.55.

The above chlorosulfonium salt (1.2 g, 6.04 mmoles) was converted into 2-methylthio-4-chloropyrrole by heating with dry xylene (20 ml) in an oxygen free atmosphere for 1/4 hour.

EXAMPLE 2B Preparation of 2-methylthio-4-chloro-5-(4-chlorobenzyl)pyrrole (Step 2x)

In a separate reaction, N,N-dimethyl-4-chlorobenzamide (1.10 g, 6.0 mmoles) was heated in a solution of dry 1,2-dichloroethane (20 ml), containing phosphorus oxychloride (0.55 ml, 6 mmoles), for 0.5 hour. (Vilsmeier-Haack reagent).

The solution containing the Vilsmeier-Haack reagent was added to the solution from Example 2A and the mixture was heated at reflux temperature in a nitrogen atmosphere for 24 hours. At this time, there was added very carefully to the coled reaction mixture a solution of sodium acetate (2 g, 30 mmoles) in water (10 ml) and the mixture was heated at reflux temperature for a further 2 hours. T.L.C. (ethyl acetate-hexane; 1:4) showed the formation of a new spot (yellow) more polar than the starting material. The solvent was removed in vacuo, water was added to the residue, the product was extracted into ethyl acetate, the extract was dried and evaporated in vacuo. The residue mostly 2-methylthio-4-chloro-5-(4-chlorobenzyl)pyrrole was subjected to column chromatography on silica gel (100 g) the product (0.787 g, 46%) being eluted with ethyl acetate-hexane (1:4). An analytical sample was prepared by crystallization from hot hexane, which yielded analytical results as follows:

mp: 142°-143° (hexane)

UV: 220, 261, 340 nm (ε 13,800, 12,300, 13,800)

IR: (CHCl₃)-- 3450, 3250, 1620 sh, 1608, 1577, 1528 cm⁻¹

NMR: (CDCl₃ --D₂ O), 2.80 (s, 3H, SCH₃), 6.57 (s, 1H, H-3), 8.00 (q, 4H, J_(AB) =8.7, H-2',3',5',6' or H-3) MS: (M+) 289, 287, 285

EXAMPLE 3 Preparation of 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio)-5-(benzoyl)pyrrole (Step 3a or 3b)

2-methylthio-5-benzoylpyrrole (0.741 g, 3.41 mmoles) was added to a suspension of 50% sodium hydride in mineral oil (0.177 g, 3.68 mmoles) in dry dimethylformamide (80 ml) maintained in an atmosphere of argon. After 1 hour at room temperature the formation of the anion was complete and compound J, spiro[2,5]-5,7-dioxa-6,6-dimethyloctane-4,8-dione (0.625 g, 3.68 mmoles) was added, and the solution was heated to 55°. After 5 hours, TLC (dioxan-dimethoxyethane acetic acid, 30:70:1) indicated that the reaction did not progress any further. The cooled solution was diluted with water (150 ml) and the starting material was extracted with ethyl acetate. The extract was dried over sodium sulfate and evaporated in vacuo to give the starting material (0.110 g, 15%). The aqueous phase from above was made acidic with 0.01 N hydrochloric acid and the product was extracted into ethyl acetate (2×100 ml). The extract was dried and evaporated in vacuo to give the crude product which was purified by column chromatography on silica gel (ethyl acetate-hexane; 1:1). There was thus obtained a solid, which after crystallization from ethyl acetate-hexane had characteristics, as indicated below of [1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methylthio)-5-(benzo yl)]pyrrole, (0.978 g. 74%) m.p. 124°-125°,

UV: (MeOH) 216, 254, 339.5 nm(ε 8510, 10,000, 14,000).

IR: (CHCl₃) 1795, 1755, 1615 cm⁻¹. NMR: (CDCl₃) 1.75 (s, 3H) 1.82 (s, 3H) 2.48 (s, 3H) 2.48-2.8 (s, 3H) 4.20 (t, 1H; J=6 Hz) 4.73 (t, 2H; J=6) 6.17 (d, 1H; J=4) 6.72 (d, 1H; J=4) 7.2-7.9 (m, 5H)

Calcd. for C₂₀ H₂₁ NO₅ S: C, 62.00; H, 5.46. Found: C, 62.01; H, 5.45.

B. In similar fashion, using the procedure outlined in A, above, and substituting for 2-methylthio-5-benzoylpyrrole the compounds listed in Example 2, part B, one obtains:

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio)-5-(benzoyl)4-n-butyl-]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio)-5-(benzoyl)4-i-propyl-]pyrrole, and

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio)-5-(benzoyl)4-methyl-]pyrrole.

C. In similar manner, using the procedure of part A of this example, and substituting for 2-methylthio-5-benzoylpyrrole the compounds listed in Example 2, part C, one obtains

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(3-thenoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(2-thenoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(3-chloro-2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(4-bromo-2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(5-methyl-2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(4-methyl-2-thenoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(1-butyl-2-pyrroyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(1-methyl-2-pyrroyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(2-pyrroyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(4-chlorobenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(3-methoxybenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(2-ethoxycarbonylbenzoyl)]-pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(2-fluorobenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(3-ethylbenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio-5-(4-ethylcarbonylbenzoyl)]-pyrrole.

EXAMPLE 3A Preparation of 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio)-4-chloro-5-(4-chlorobenzoyl)pyrrole (Step 3a, 3b)

Sodium hydride in mineral oil (50%, 0.686 g, 14.3 mmoles) was added to a solution of the 2-methylthio-4-chloro-5-(4-chlorobenzoyl)pyrrole prepared in Example 2B compound (4.1 g, 14.3 mmoles) in dry dimethylformamide (44 ml) maintained in a nitrogen atmosphere. After 40 minutes spiro [2,5]-5.7-dioxa-6,6-dimethyloctane-4,8-dione (2.43 g, 14.3 mmoles) was added and the temperature was heated slowly to 70° and maintained three for 3 hours. The cooled solution was added slowly to ether (880 ml) with good agitation and the sodium salt of 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio)-4-chloro-5-(4-chlorobenzoyl)pyrrole which precipitated (6.78 g, 99%) was collected by filtration, washed with ether, and dried in vacuo, and used as such in Example 12A.

EXAMPLE 4 Preparation of [1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl] -2-methanesulfonyl)-5-(benzoyl)]pyrrole (Step 4b)

To a solution of [1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio)-5-(benzoyl)]pyrrole (0.500 g, 1.29 mmoles) in dry dichloromethane (100 ml), cooled in an ice bath, was added 85% m-chloroperbenzoic acid (0.600 g, 3.47 mmoles). The reaction was followed by TLC (ethyl acetate-hexane); 1:1 on silica gel. Two spots, more polar than the starting material, were observed. The most polar corresponded to the sulfoxide and the other to the sulfone. After three hours at this temperature, the solvent was evaporated in vacuo, and the solid residue was washed with ether to remove m-chlorobenzoic acid to leave a solid (0.486 g, 90%) with m.p. 154°-155° (dec.). After crystallization from aqueous acetone the product was shown to be, [1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(benzoyl)-pyrrole, m.p. 159° (dec.).

UV: (MeOH) 260, 292, nm (ε10,200, 16,900).

IR: (KBr) 1787, 1742, 1645 cm⁻¹.

NMR: (DMSO d₆) or (Pyridine d₅), 1.67 (s, 6H), 3.05 (t, 2H; J=6.5 Hz), Pyridine-d₅, 3.60 (s, 3H) 5.32 (t, 2H; J=6.5), 6.62 (d, 1H; J=4) DMSO-d₆, 6.83 (d, 1H; J=4), 7.4-7.9 (m, 5H).

The methine proton was not clearly visible in either solvent.

Calcd. for C₂₀ H₂₁ NO₇ S: C, 57.28; H, 5.05; N, 3.34. Found: C, 57.20; H, 5.25; N, 3.29.

B. Similarly, substituting for 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methy(-lthio)-5-(benzoyl)pyrrole the compounds of Example 3, part B, one obtains

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-4-(n-butyl)-5-(benzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-4-(i-propyl)-5-(benzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-4-(methyl)-5-(benzoyl)]pyrrole.

C. Substituting for 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methylthio)-5-(benzoyl)pyrrole the compounds of Example 3, part C, one obtains:

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(3-thenoyl)pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl]ethyl]-2-(methanesulfonyl)-5-(2-thenoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(3-chloro-2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(4-bromo-2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(5-methyl-2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(4-methyl-2-thenoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(1-butyl-2-pyrroyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(1-methyl-2-pyrroyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(2-pyrroyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(4-chlorobenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(3-methoxybenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(2-ethoxycarbonylbenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(2-fluorobenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(3-ethylbenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(4-ethylcarbonylbenzoyl)]pyrrole.

EXAMPLE 5 Preparation of [1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl)-5-(benzoyl)pyrrole (Steps 5b, 5c)

To a solution of [1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(benzoyl)]pyrrole (0.419 g) in methanol (25 ml) was added methanol (25 ml) which had been saturated with hydrogen chloride gas. The resultant mixture was heated at reflux for 0.5 hour, the progress of reaction being followed by TLC (ethyl acetate-hexane; 1:3) on silica gel. The solvent was removed in vacuo and the residue was percolated through a column of silica gel using ethyl acetate-hexane (1:4) as the percolating solvent. A viscous oil [1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl)-5-(benzoyl)]-pyrrole (0.386 g, 95%) was obtained.

UV: (MeOH) 220, 261, 292.5 nm (ε7590, 10,700 1590).

IR: (CHCl₃) 1755, 1740, 1650 cm⁻¹.

NMR: (CDCl₃). 2.48 (m, 2H), 3.22 (s, 3H), 3.55 (t, 1H), 3.72 (s, 6H), 4.80 (m, 2H), 6.67 (d, 1H; J=4 Hz), 6.88 (d, 1H; J=4), 7.3-7.9 (m, 5H),

Calcd. for C₁₉ H₂₁ NO₇ S: C, 56.01; H, 5.19; N, 3.43. Found: C, 55.87; H, 5.25; N, 3.24.

B. Substituting into the procedure of Part A for 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methanesulfonyl)-5-(benzoyl)pyrrole the compounds listed in Example 4, part B, one obtains:

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-4-(n-butyl)-5-benzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-4-(i-propyl)-5-benzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-4-(methyl)-5-benzoyl)]pyrrole.

C. Substituting into the procedure of Part A for 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methanesulfonyl)-5-(benzoyl)pyrrole the compounds listed in Example 4, part C, one obtains:

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(3-thenoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(2-furoyl)]pyrrole

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(2-thenoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(3-chloro-2-furoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(4-bromo-2-furoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(5-methyl-2-furoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(4-methyl-2-thenoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(1-butyl-2-pyrroyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(1-methyl-2-pyrroyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(2-pyrroyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(4-chlorobenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(3-methoxybenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(2-ethoxycarbonylbenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(2-fluorobenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(3-ethylbenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methanesulfonyl)-5-(4-ethylcarbonylbenzoyl)]pyrrole.

EXAMPLE 6 Preparation of 2-methylsulfonyl-5-benzoylpyrrole (Step 3c)

A. A solution of 2-methylthio-5-benzoylpyrrole (0.300 g, 1.38 mmoles) and m-chloroperbenzoic acid (0.550 g; 86%, 3.18 mmoles) in anhydrous dichloromethane (50 ml) was stirred at 5° C. for 3 hours. The solution was extracted with 20% sodium carbonate solution, the organic phase was separated, dried over sodium sulfate and evaporated in vacuo. The residue was crystallized from acetone-hexane 2-methylsulfonyl-5-benzoylpyrrole (0.320 g, 100%)

mp: 148°-150° (acetone-hexane)

UV: 258, 294 nm (ε8710, 16,600)

IR: (CHCl₃) 11047, 3565, 3410, 3255, 1640, 1604, 1580 cm⁻¹

NMR: (CDCl₃), 3.22 (s, 3H), 6.86 (s, 1H), 6.90 (s, 1H), 7.40-7.60 (m, 3H), 7.82-8.00 (m, 2H), 11.10 (s, 1H, W_(H) =16 Hz).

MS: 249 (M⁺)

Calcd. for C₁₂ H₁₁ No₃ S: C, 57.81; H, 4.45; N, 5.60. Found: C, 57.85; H, 4.44; N, 5.57

B. Similarly, substituting into the procedure of part A for 2-methylthio-5-benzoylpyrrole the compounds listed in Example 2, part B, one obtains:

2-methylsulfonyl-4-n-butyl-5-benzoylpyrrole,

2-methylsulfonyl-4-i-propyl-5-benzoylpyrrole, and

2-methylsulfonyl-4-methyl-5-benzoylpyrrole.

C. Similarly, substituting into the procedure of part A for 2-methylthio-5-benzoylpyrrole the compounds listed in Example 2, part C, one obtains:

2-methylsulfonyl-5-(3-thenoyl)pyrrole,

2-methylsulfonyl-5-(2-furoyl)pyrrole,

2-methylsulfonyl-5-(2-thenoyl)pyrrole,

2-methylsulfonyl-5-(3-chloro-2-furoyl)pyrrole,

2-methylsulfonyl-5-(4-bromo-2-furoyl)pyrrole,

2-methylsulfonyl-5-(5-methyl-2-furoyl)pyrrole,

2-methylsulfonyl-5-(4-methyl-2-thenoyl)pyrrole,

2-methylsulfonyl-5-(1-butyl-2-pyrroyl)pyrrole,

2-methylsulfonyl-5-(1-methyl-2-pyrroyl)pyrrole,

2-methylsulfonyl-5-(2-pyrroyl)pyrrole,

2-methylsulfonyl-5-(4-chlorobenzoyl)pyrrole,

2-methylsulfonyl-5-(3-methoxybenzoyl)pyrrole,

2-methylsulfonyl-5-(2-ethoxycarbonylbenzoyl)pyrrole,

2-methylsulfonyl-5-(2-fluorobenzoyl)pyrrole,

2-methylsulfonyl-5-(3-ethylbenzoyl)pyrrole,

2-methylsulfonyl-5-(4-ethylcarbonylbenzoyl)pyrrole.

EXAMPLE 7 Preparation of 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methanesulfonyl)-5-(benzoyl)pyrrole (Step 4c)

A. To a stirred suspension of 50% sodium hydride in mineral oil (1.56 g, 48 mmoles) in dry dimethylformamide (100 ml), maintained in an atmosphere of nitrogen, was added the sulfone 2-methylsulfonyl-5-benzoylpyrrole (12.0 g, 48 mmoles), dissolved in dry dimethylformamide (30 ml), over a 5 minute period. When gas evolution had ceased, the cyclopropyl compound spiro[2,5]-5,7-dioxa-6,6-dimethyloctane-4,8-dione (8.16 g, 48 mmoles) was added and the solution was heated at 90° for 4 hours. The cooled solution was diluted with 10% hydrochloric acid solution and the resultant was extracted with ethyl acetate. The extract was washed with water, dried over sodium sulfate and evaporated in vacuo. The residue was subjected to column chromatography on silica gel (600 g) using ethyl acetate-hexane (2:3) as the eluting solvent. In this way there was obtained the starting sulfone (3.0 g, 25%) and the product 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-methanesulfonyl)-5-(benzoyl)pyrrole (7.0 g, 35%; 46% based on starting material consumed). Recrystallization of the product was effected from aqueous acetone.

mp: 155°-156° (water-acetone).

UV: 260, 292 nm (ε10,200, 17,000).

IR: (KBr) 1780, 1746, 1649 cm⁻¹

NMR: (Pyridine-d₅), 1.62 (s, 3H), 3.02 (5, 2H, J=6.8 Hz), 3.57 (s, 3H), 5.28 (5, 2H, J=6.8 Hz), 6.58 (d, 1H, J=4.1 Hz), 7.03 (d, 1H, J=4.1 Hz), 7.33-7.51 (m, 3H), 7.77-7.94 (m, 2H).

Calcd. for C₂₀ H₂₁ No₇ S: C, 57.28; H, 5.05; N, 3.34. Found: C, 57.20; H, 5.25; N, 3.29.

B. Similarly substituting into the procedure of part A for 2-methylsulfonyl-5-benzoylpyrrole the compounds listed in Example 6, part B, one obtains:

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-4-(n-butyl)-5-(benzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-4-(i-propyl)-5-(benzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-4-(methyl)-5-(benzoyl)]pyrrole.

C. Similarly, substituting into the procedure of part A for 2-methylsulfonyl-5-benzoylpyrrole the compounds listed in Example 6, Part C, one obtains:

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(3-thenoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(2-thenoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(3-chloro-2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-b 5-yl)ethyl]-2-(methanesulfonyl)-5-(4-bromo-2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(5-methyl-2-furoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(4-methyl-2-thenoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(1-butyl-2-pyrrol)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(1-methyl-2-pyrroyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(2-pyrroyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(4-chlorobenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(3-methoxybenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(2-ethoxycarbonylbenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(2-fluorobenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(3-ethylbenzoyl)]pyrrole,

[1-[2-(4,6-dioxo-2,2-dimethyl-1,3-dioxan-5-yl)ethyl]-2-(methanesulfonyl)-5-(4-ethylcarbonylbenzoyl)]pyrrole.

EXAMPLE 8 Preparation of dimethyl 5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate (Step 6)

Sodium hydride in mineral oil (50%, 0.060 g, 1.2 mmoles) was added to a solution of [1-[3,3-(dimethoxycarbonyl) -propyl]-2-methanesulfonyl)-5-(benzoyl)]pyrrole (0.463 g, 1.13 mmoles) in dry dimethylformamide (25 ml) in a nitrogen atmosphere. After 0.5 hour at room temperature the solution was heated, in an oil bath, at 100°-110° for 2 hours. The progress of the reaction was followed by TLC (ethyl acetate-hexane; 1:3) on silica gel. The solution was cooled to room temperature, water (100 ml) was added, and the solution was made acidic with 0.01N hydrochloric acid. The products were extracted into ethyl acetate (total of 100 ml), the extract was dried and evaporated in vacuo. Ethereal diazomethane was added to the residue and after removal of the ether and excess diazomethane in vacuo the mixture of esters was subject to column chromatography on silica gel using ethyl acetate-hexane (1:3) as the eluting solvent. In this way there was isolated a mixture of dimethyl 5 -benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate and methyl 5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylate acid as an oil (0.210 g) [and starting material (0.097 g, 21%], which was normally used without purification in the next step. The two esters, could, however, be separated by TLC on silica gel using ethyl acetate hexane (1:4) as the developing solvent.

For dimethyl 5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1,1-dicarboxylate

IR: (CHCl₃) 1745, 1740, 1620, 1575(w) cm⁻¹.

NMR: (CDCl₃), 3.00 (t, 2H; J=6.4 Hz), 3.63 (s, 6H), 4.36 (t, 2H, J=6.4), 6.04 (d, 1H, J=4), 6.56 (d, 1H; J=4), 7.00-7.57 (m, 5H).

The methyl 5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1-carboxylate was also an oil and physical properties essentially identical to an authentic sample prepared by another route.

Calcd. for C₁₉ H₂₁ NO₇ S: C, 56.01; H, 5.19; N, 3.43. Found: C, 55.87; H, 5.25; N, 3.24.

B. Similarly, substituting into the procedure of part A for 1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl)-5-(benzoyl)pyrrole the compounds listed in Example 5, part B, one obtains:

dimethyl 4-n-butyl-5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 4-i-butyl-5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 4-methyl-5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate.

C. Similarly, substituting into the procedure of Part A for 1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl)-5-(benzoyl)pyrrole the compounds listed in Example 5, part C, one obtains:

dimethyl 5-(3-thenoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(2-furoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1,1-dicarboxylate,

dimethyl 5-(2-thenoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(3-chloro-2-furoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(4-bromo-2-furoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(5-methyl-2-furoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(4-methyl-2-thenoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(1-butyl-2-pyrroyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(1-methyl-2-pyrroyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(2-pyrroyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(4-chlorobenzoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(3-methoxybenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(2-ethoxycarbonylbenzoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(2-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate,

dimethyl 5-(3-ethylbenzoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate

dimethyl 5-(4-ethylcarbonylbenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate.

EXAMPLE 9 Preparation of 5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylic acid Decarboxylation of dimethyl 5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1,1-decarboxylate and simultaneous hydrolysis of methyl 5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylate

A. A mixture of two esters (0.273 g) was heated at reflux temperature in water (1 ml) methanol (3 ml) solution with six equivalents of potassium hydroxide for 0.5 hour. The solvent was removed in vacuo, water (50 ml) was added and the solution was made acidic with 10% hydrochloric acid. The product was extracted with ethyl acetate, the extract was washed with water, dried over sodium sulfate, and evaporated in vacuo. The solid residue (0.232 g, 85%) had m.p. 158° and was identical to an authentic specimen of 5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylic acid prepared by another route.

B. Similarly, substituting into the procedure of part A for dimethyl 5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate the compounds listed in Example 8, part B, one obtains:

4-n-butyl-5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylic acid,

4-i-propyl-5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylic acid,

4-methyl-5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylic acid.

C. Similarly, substituting into the procedure of part A for dimethyl 5-benzoyl-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate the compounds listed in Example 8, part C, one obtains.

5-(3-thenoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrolo-1-carboxylic acid,

5-(2-furoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrolo-1-carboxylic acid,

5-(2-thenoyl)-1,2-dihydro-3H-pyrrolo[1,2a]pyrrolo-1-carboxylic acid,

5-(3-chloro-2-furoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrolo-1-carboxylic acid,

5-(4-bromo-2-furoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrolo-1-carboxylic acid,

5-(5-methyl-2-furoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrolo-1-carboxylic acid,

5-(4-methyl-2-thenoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrolo-1-carboxylic acid,

5-(1-butyl-2-pyrroyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrolo-1-carboxylic acid,

5-(1-methyl-2-pyrroyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrolo-1-carboxylic acid,

5-(2-pyrroyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrolo-1-carboxylic acid,

5-(4-chlorobenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrolo-1-carboxylic acid,

5-(3-methoxybenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrolo-1-carboxylic acid,

5-(2-ethoxycarbonylbenzoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]-pyrrolo-1-carboxylic acid,

5-(2-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrolo-1-carboxylic acid,

5-(3-ethylbenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrolo-1-carboxylic acid,

5-(4-ethylcarbonylbenzoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]-pyrrolo-1-carboxylic acid.

EXAMPLE 10 Preparation of 2-(methylthio)-5-(4-fluorobenzoyl)pyrrole (Step 2)

A solution of N,N-dimethyl-4-fluorobenzamide (8.4 g, 0.05 moles) in anhydrous 1,2-dichloroethane (170 ml) containing phosphorus oxychloride (7.7 g, 0.05 moles) was heated at reflux temperature for 1 hour. At the end of this time 2-methylthiopyrrole (2.82 g, 0.025 moles) was added and heating was continued for an additional 0.5 hour. The solution was cooled to room temperature, and to the cooled solution was cautiously added, with good agitation, a solution of sodium acetate (12.3 g, 0.15 moles) in water (50 ml) and the mixture was then boiled under reflux for 1 hour. The organic phase was separated, washed with water, dried, and evaporated. The residue was subjected to column chromatography on silica gel suing ethyl acetate-hexane (1:9) as the eluting solvent. A yellow colored solid 2-(methylthio)-5-(4-fluorobenzoyl)pyrrole (3.2 g, 54%) was obtained which after crystallization from ether-hexane had m.p. 112°-113° C.

UV: (MeOH) 218.5, 248, 343 nm (ε9770, 8510, 13,800).

IR: (CHCl₃) 3440, 3250, 1610 cm⁻¹.

NMR: (CDCl₃), 2.48 (s, 3H), 6.25 (q, 1H; J=2.5, 4 Hz), 6.80 (q, 1H; J=2.5, 4 Hz), 7.12 (q, 2H; J=8, 8), 7.92 (q, 2H; J=5.5, 8), 10.67 (s, 1H; WH=22).

Calcd. for C₁₂ H₁₀ FNOS: C, 61.24; H, 4.28. Found: C, 61.01; H, 4.21.

EXAMPLE 11 Preparation of 1-[[2-(4,6-dioxo-2,2-dimethyl-1,3-benzodioxan-5-yl)ethyl]-2-(methylthio)-5-(4-fluorobenzoyl)pyrrole (Step 3a or 3b)

A (0.227 g, 0.97 mmoles) was added to a suspension of 50% sodium hydride in mineral oil (0.054 g, 1.0 mmoles) in dry dimethylformamide (15 ml) 2-(methylthio)-5-(4-fluorobenzoyl)pyrrole and stirred at room temperature, in an argon atmosphere for 0.5 hour. Compound J, spiro[2,5]-5,7-dioxa-6,6-dimethyloctane-4,8-dione (0.181 g, 1.07 mmoles) was then added and the mixture was heated in an oil bath at 65° for 1.4 hours. The solution was cooled to room temperature, water (150 ml) was added and the starting material was extracted into ethyl acetate. The extract was washed with water, dried over sodium sulfate and evaporated in vacuo to give the unconsumed reactant (0.050 g, 22%). The aqueous phase from above was made acidic with 0.01N hydrochloric acid, the products were extracted into ethyl acetate and the extract was dried and evaporated. The residue (0.434 g) was subjected to column chromatography on silica gel using ethyl acetate-hexane-methanol (9:10:1) as the eluting solvent. The product (0.284 g, 56%) and a slightly more polar substance (0.030 g) were isolated. In another reaction, using the same conditions, but a freshly opened can of sodium hydride, a 72% yield of the desired product was obtained.

Crystallization of the product from ethyl acetate hexane gave material 1-[[2-(4,6-dioxo-2,2-dimethyl-1,3-benzodioxan-5-yl)ethyl]-2-(methylthio)-5-(4-fluorobenzoyl)]pyrrole m.p. 92°, which was isolated as the monohydrate.

UV: (MeOH) 217, 265.5, 340 μm (μ5370, 8130, 7760).

IR: (CHCl₃) 1795, 1755, 1620 1600 cm⁻¹.

NMR: (CDCl₃). 1.77 (s, 3H), 1.82 (s, 3H), 2.50 (s, 3H), 2.4-2.8 (m, 2H), 4.15 (t, 1H; J=5.5 Hz), 4.70 (t, 2H; J=6), 6.17 (d, 1H; J=4), 6.68 (d, 1H; J=4), 7.05 (q, 2H; J=8,8), 7.72 (q, 2H; J=6,8),

Calcd. for C₂₀ H₂₀ FNO₅ S H₂ O: C, 56.72; H, 5.24; N, 3.31. Found: C, 56.84; H, 5.15; N, 3.24.

EXAMPLE 12 Preparation of [1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(4-fluorobenzoyl)pyrrole (Step 4a)

To a solution of 1-[[2-(4,6-dioxo-2,2-dimethyl-1,3-benzodioxan-5-yl)ethyl]-2-(methylthio)-5-(4-fluorobenzoyl)]pyrrole (0.50 g) in methanol (15 ml) was added methanol which had been saturated with hydrogen chloride gas (15 ml). The solution was heated at reflux temperature for 0.5 hour and the solvent was then removed in vacuo. The residue was then percolated through a column of silica gel using ethyl acetate-hexane (1:4) as the percolating solvent. The produce [1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(4-fluorobenzoyl)-pyrrole was obtained as an oil.

UV: (MeOH) 215, 248, 334 nm (ε 10,000, 8510, 14,500).

IR: (CHCl₃) 1755, 1735, 1620, 1600 cm⁻¹.

MS: 393 (M⁺).

NMR: (CDCl₃), 2.47 (s, 3H), 2.20-2.65 (m, 2H), 3.48 (t, 1H; J=7 Hz), 3.72 (s, 6H), 4.58 (t, 2H; J=7), 6.17 (d, 1H; J=4), 6.67 (d, 1H; J=4) 7.07 (q, 2H; J=8,5, 8.5), 7.75 (q, 2H; J=5.5, 8.5).

B. Similarly, substituting into the procedure of part A for 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-benzodioxan-5yl)-ethyl]-2-(methylthio)-5-(4-fluorobenzoyl)pyrrole the compounds listed in Example 3, part B, one obtains:

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-4-(n-butyl)-5-(benzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-4-(i-propyl)-5-(benzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-4-(methyl)-5-(benzoyl)]pyrrole.

C. Similarly, substituting into the procedure of part A for 1-[2-(4,6-dioxo-2,2-dimethyl-1,3-benzodioxan-5yl)-ethyl]-2-(methylthio)-5-(4-fluorobenozyl)pyrrole the compounds listed in Example 3, part C, one obtains:

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(3-theonyl)]-pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(2-furoyl)-]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(2-theonyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(3-chloro-2-furoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(4-bromo-2-furoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(5-methyl-2-furoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(4-methyl-2-thenoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(1-butyl-2-pyrroyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(1-methyl-2-pyrroyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(2-pyrroyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(4-chlorobenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(3-methoxybenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(2-ethoxycarbonylbenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(2-fluorobenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(3-ethylbenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(4-ethylcarbonylbenzoyl)]pyrrole.

EXAMPLE 12A Preparation of [1-[3,3-(dimethoxycarbonyl)propyl]-2-methylthio-4-chloro-5-(4-chlorobenzoyl)]pyrrole (Step 4a)

The crude salt prepared in Example 3A was dissolved in methanol (100 ml) and a saturated solution of hydrogen chloride in methanol (150 ml) was added and the solution was left at room temperature for 12 hours. The solution was evaporated in vacuo at 25° C. and the oil which remained was subjected to column chromatography on silica gel (350 g) using dichloromethane as the eluting solvent. Removal of the solvent in vacuo gave the [1-[3,3-(dimethoxycarbonyl)propyl]-2-methylthio-4-chloro-5-(4-chlorobenzoyl)]pyrrole (3.25 g, 51%) as a yellow oil. mp: oil.

UV: 213, 266, 338 nm (ε 14,800, 14,100, 11,800).

IR: (CHCl₃) 1757, 1738, 1625, 1528 cm⁻¹

NMR: (CDCl₃ T-60), 2.24 (m, 2H, CH₃), 2.49 (s, 3H, SCH₃), 3.47 (t, 1H, J=7.2, CH), 3.77 (s, 6H, OCH₃), 4.16 (m, 2H, NCH₂), 6.21 (s, 1H, H-3), 7.65 (q, 4H, J_(AB) =8.6, H-2', 3', 5', 6').

MS: (M+) 447, 445, 443.

Calcd. for C₁₉ Cl₂ NO₅ S: C, 51.36; H, 4.31; N, 3.15. Found: C, 51.61; H, 4.39; N, 3.08.

EXAMPLE 13 Preparation of [1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(4-fluorobenzoyl)-pyrrole (Step 5a)

A. A solution of [1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(4-fluorobenzoyl)]pyrrole (0.700 g, 1.5 mmoles) in dry dichloromethane (50 ml) containing 85% m-chloroperbenzoic acid (0.700 g. 4 mmoles) was cooled in an ice bath and after 1 hours TLC (dimethylethane-dioxan-acetic acid, 70:30:1) indicated that only the sulfone [1-[3,3-(dimethoxycarbonyl)-propyl]-2-methanesulfonyl-5-(4-fluorobenzoyl)]pyrrole was present. The solvent was removed in vacuo, the residue was shaken with 10% sodium bicarbonate solution and the product was extracted into ether. The extract was washed with water, dried, and evaporated. The residue was subjected to column chromatography on silica gel using ethyl acetate-hexane (3:7) as the eluant. The product, [1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(4-fluorobenzoyl)]pyrrole, was obtained as an oil (0.558 g, 80%).

UV: (MeOH) 219, 259, 291.5 nm (ε 8510, 8710, 13,500).

IR: (CHCl₃) 1755, 1735, 1650, 1600, 1325, 1145, 1125 cm⁻¹.

NMR: (CDCl₃), 2.42 (m, 2H), 3.23 (s, 3H), 3.4-3.8 (m, 1H), 3.75 (s, 6H), 4.78 (m, 2H), 6.65 (d, 1H; J=4 Hz), 6.92 (d, 1H; J=4), 6.95-8.10 (m, 4H).

Calcd. for C₁₉ H₂₀ FNO₇ S: C, 53.64; H, 4.74; N, 3.29. Found: C, 53.82; H, 4.91; N, 3.06.

B. Similarly, substituting into the procedure of part A for 1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(4-fluorobenozyl)pyrrole the compounds listed in Example 12, part B, one obtains:

[1[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-4-n-butyl-5-benzoyl]pyrrole,

[1[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-4-i-propyl-5-benzoyl]pyrrole,

[1[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-4-methyl-5-benzoyl]pyrrole.

C. Similarly, substituting into the procedure of part A for 1-[3,3-(dimethoxycarbonyl)propyl]-2-(methylthio)-5-(4-fluorobenzoyl)pyrrole one obtains:

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(3-thenoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(2-furoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(2-thenoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(3-chloro-2-furoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(4-bromo-2-furoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(5-methyl-2-furoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(4-methyl-2-thenoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(1-butyl-2-pyrroyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(1-methyl-2-pyrroyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(2-pyrroyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(4-chlorobenzoyl)]-pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(3-methoxybenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(2-ethoxycarbonylbenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbonyl)propyl]-2-methanesulfonyl-5-(2-fluorobenzoyl)]pyrrole,

[1-[3,3-(dimethoxycarbony)propyl]-2-methanesulfonyl-5-(3-ethylbenzoyl)]pyrrole, [1-[3,3-(dimethoxycarbonyl)propyl]-2-methansulfonyl-5-(4-ethylcarbonylbenzoyl)]pyrrole.

EXAMPLE 13A Oxidation to the sulfone (Step 5a)

A solution of m-chloroperbenzoic acid (86%, 4.11 g, 23.6 mmoles) in dichloromethane (200 ml) was added dropwise with stirring to a solution of the methylthio derivative of Example 12A (2.90 g, 6.54 mmoles) in dichloromethane (100 ml). After 2.5 hours the solvent was removed in vacuo and the residue was shaken with 5% sodium bicarbonate solution. Dichloromethane was added, the mixture was shaken and the organic phase was separated, dried and evaporated in vacuo. The crude product was percolated through a column of silica gel (120 g) using ethyl acetate/hexane (3:7) as the percolating solvent. Evaporation of the solvent gave the [1-(3,3-dimethoxycarbonyl)propyl]-2-methanesulfonyl-4-chloro-5-(4-chlorobenzoyl)]pyrrole (2.95 g, 95%) which was crystallized from dichloromethane-hexane for analysis.

mp: 127°.

UV: 211, 229, 275 nm (ε 10,000, 11,800, 15,900).

IR: (CHCl₃) 1756, 1738, 1749, 1589, 1574 cm⁻¹.

NMR: (CDCl₃).

2.33 (m, 2H, (CH₂), 3.24 (s, 3H, SO₂ CH₃), 3.50 (t, 1H, J=7.2, CH), 3.73 (s, 6H, OCH₃), 4.58 (m, 2H, NCH₂), 6.92 (s, 1H, H-3), 7.70 (q, 4H, J_(AB) =8.7, H-2', 3', 5', 6'),

MS: (M+) 477,475.

Calcd. for C₁₉ H₁₉ Cl₂ NOS: C, 47.90; H, 4.02; N, 2.94. Found: C, 47.97; H, 3.98; N, 2.87.

EXAMPLE 14 Preparation of dimethyl 5-(4-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate (Step 6)

Sodium hydride in mineral oil (50%, 0.048 g, 1 mmol) was added, under a nitrogen atmosphere, to a solution of (0.483 g, 0.8 mmoles) in dry dimethylformamide (30 ml). After 1 hour at room temperature, the reaction was placed in an oil bath at 90° for 4 hours. The reaction progress was follwed by TLC on silica gel (ethyl acetate-hexane; 1.3). Water was added to the cooled solution and the product was extracted with ethyl acetate. The extract was washed with water, dried and evaporated. The residue was treated with excess ethereal diazomethane and after removal of the solvent the product mixture was subjected to column chromatography on silica gel using ethyl acetate-hexane (1:4) as the eluting solvent. In this way an oily mixture of dimethyl 5-(4-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate and methyl 5-(4-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1-carboxylate (0.145 g) and the starting material (0.080 g, 23%) were obtained.

EXAMPLE 14A Preparation of dimethyl 5-(4-chlorobenzoyl)-6-chloro-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate (Step 6)

The sulfone from Example 13A (2.0 g, 4.2 mmoles) was added to a stirred suspension of 50% sodium hydride in mineral oil (0.220 g, 4.4 mmoles) in dry dimethyl formamide (35 ml) maintained in a nitrogen atmosphere. The appearance of gas bubbles and an intense orange color indicated the formation of the anion. When gas evolution has ceased the solution heated to 60° in an oil bath for 4 hours. Water was then added to the cooled solution and the product was extracted into ethyl acetate. The extract was washed with water, dried over sodium sulfate and evaporated in vacuo. The residue was chromatographed on a column of silica gel (100 g/g substrate) using ethyl acetate-hexane (1:4) as the eluting solvent. The desired product was obtained as a solid dimethyl 5-(4-chlorobenzoyl)-6-chloro-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1,1-dicarboxylate (1.33 g, 80%) which was crystallized from ether-hexane for analysis.

mp: 127°-128°.

UV: 215, 264, 309 nm (ε 12,000, 11,200, 15,800).

IR: (CHCl₃) 1757, 1625, 1596 cm⁻¹.

NMR: (CDCl₃), 3.09 (t, 2H, J=7.1, CH₂), 3.86 (s, 6H, OCH₃), 4.49 (t, 2H, J=7.1, NCH₂), 6.33 (s, 1H, H-7), 7.62 (q, 4H, J_(AB) =8.4, H-2', 3', 5', 6'),

MS: (M+) 399,397,395.

Calcd. for C₁₈ H₁₅ Cl₂ NO₅ : C, 54.54; H, 3.81; N, 3.53. Found: C, 54.68; H, 3.81; N, 3.43.

EXAMPLE 15 Preparation of 5-(4-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1-carboxylic acid: Decarboxylation of dimethyl 5-(4-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate and simultaneous hydrolysis of methyl 5-(4-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylate (Decarboxylation step)

A solution of the mixture of dimethyl 5-(4-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1,1-dicarboxylate and methyl 5-(4-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylate (0.200 g) in methanol (5 ml) and water (3 ml) containing potassium hydroxide (0.5 g) was heated at reflux temperature for 1 hour. The solvent was removed in vacuo, water was added to the residue and the solution waas made acidic with 10% hydrochloric acid solution. The product was extracted into ethyl acetate, the extract was dried and evaporated. The solid residue on crystallization from ethyl acetate-hexane gave 5-(4-fluorobenzoyl)-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid (0.124 g, 80%) m.p. 163°. A mixed m.p. with an authentic specimen (m.p. 170°) had m.p. 165°. The IR spectrum was identical to that of the authentic sample.

EXAMPLE 15A Preparation of 5-(4-chlorobenzoyl)-6-chloro-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid (Decarboxylation Step)

A solution of the diester from Example 14A (0.500 g, 1.26 mmoles) in methanol (10 ml) and water (3 ml) containing sodium hydroxide (0.300 g, 7.5 mmoles) was heated at reflux temperature for 0.5 hour. The methanol was removed in vacuo, water was added, and the solution was made acidic with 3N hydrochloride acid. The product was extracted into ether, the ether was washed with water, dried, and evaporated. The nearly white solid which remained (0.380 g, 93%), after washing with a little cold ether, had m.p. 197° which was undepressed on admixture with a sample of 5-(4-chlorobenzoyl)-6-chloro-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid prepared by another route.

EXAMPLE 15B

Following the sequence of reactions in Examples 1A, 2A, 2B, 3A, 12A, 13A, 14A and 15A are prepared:

5-(3-thenoyl)-6-chloro-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1-carboxylic acid;

5-(2-furoyl)-6-chloro-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1-carboxylic acid;

5-(5-chloro-2-furoyl)-6-chloro-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylic acid;

5-(4-ethoxycarbonylbenzoyl)-6-chloro-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylic acid;

5-(4-bromobenzoyl)-6-bromo-1,2-dihydro-3H-pyrrolo-[1,2-a]pyrrole-1-carboxylic acid;

5-(2,4-dimethylbenzoyl)-6-bromo-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid;

5-(3-methyl-2-furoyl)-6-bromo-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid;

5-(3,5-dimethoxybenzoyl)-6-chloro-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid;

5-(3-chloro-2-thenoyl)-6-chloro-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid;

5-(4-methyl-2-thenoyl)-6-bromo-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid;

5-(1-n-butyl-2-pyrrolyl)-6-chloro-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid; and

5-(3,5-dimethylcarbonylbenzoyl)-6-chloro-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid. 

What is claimed is:
 1. A compound of the formula ##STR12## wherein: X is chloro or bromo; Ar is a moiety selected from the group consisting of ##STR13## in which: Y is oxygen or sulfur;R is hydrogen, methyl, chloro, or bromo; R¹ is hydrogen, lower alkyl of one to four carbon atoms, lower alkoxyl of one to four carbon atoms, carboxyl, lower alkoxycarbonyl in which the alkoxy group has one to four carbon atoms, lower alkylcarbonyl in which the alkyl group has one to four carbon atoms, fluoro, chloro or bromo; R² is hydrogen or lower alkyl of one to four carbon atoms; and each R³ is independently hydrogen or lower alkyl of one to four carbon atoms.
 2. The compound of claim 1 wherein X is chloro, and Ar is 2-thenoyl, 2-furoyl, 2-pyrroyl or phenyl substituted with R¹ as is defined in claim
 1. 